New tech measures arm precision in shoulder patients
NCT ID NCT07133100
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study will test a system called AuReha to see how well it measures arm movement precision in people with shoulder issues like instability or stiffness. About 52 adults will do exercises with both their healthy and affected arms, and the system will track movement accuracy, trunk stability, and more. The goal is to understand if the system can reliably detect differences between the two arms, which could help in future rehabilitation.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 52 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Oct 2025
An estimate. Start dates often move.
- Expected to finish
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Oct 2025
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * patients with a healthy contralateral limb * patients affected by orthopedic shoulder conditions such as posterior instability, anterior instability, anterior Latarjet instability, adhesive capsulitis, or prostheses * age ≥18 years * patients who consent to participate in the study by signing the informed consent form Exclusion Criteria: * Pregnant and/or breastfeeding women (verified through self-declaration) * Epilepsy * Allergy or hypersensitivity to materials used in the medical device, specifically: polypropylene and lycra (fabric), nylon (integrated zipper), viscose and elastane (zipper integration fabric) * Chronic headache under treatment
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Poliambulatorio Shoulder Team
Forlì, FC, 47122, Italy
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Other studies related to the condition(s) this trial covers.
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